A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750895



Internal ID20526755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33746819..33746819hg38UCSC Ensembl
chr13:34320956..34320956hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259971
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750895
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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